Meiotic origin of trisomy in confined placental mosaicism is correlated with presence of fetal uniparental disomy, high levels of trisomy in trophoblast, and increased risk of fetal intrauterine growth restriction.

Uniparental disomy in humans: development of an imprinting map and its implications for prenatal diagnosis

1995 • 410 citations

Chromosomal Mosaicism Confined to the Placenta in Human Conceptions

1983 • 387 citations

Uniparental disomy 7 in Silver—Russell syndrome and primordial growth retardation

1995 • 299 citations

Recombination and maternal age-dependent nondisjunction: molecular studies of trisomy 16.

1995 • 224 citations

Confirmation of CVS mosaicism in term placentae and high frequency of intrauterine growth retardation association with confined placental mosaicism

1991 • 199 citations

Uniparental disomy for chromosome 16 in humans.

1993 • 190 citations

CONFINED PLACENTAL MOSAICISM FOR TRISOMIES 2, 3, 7, 8, 9, 16, AND 22: THEIR INCIDENCE, LIKELY ORIGINS, AND MECHANISMS FOR CELL LINEAGE COMPARTMENTALIZATION

1996 • 187 citations

Relationship between homozygosity at the dopamine D3 receptor gene and schizophrenia

1994 • 179 citations

Placental mosaicism and intrauterine survival of trisomies 13 and 18.

1989 • 179 citations

Trisomy 15 with loss of the paternal 15 as a cause of Prader-Willi syndrome due to maternal disomy.

1992 • 171 citations

Confined chorionic mosaicism in prenatal diagnosis

1987 • 156 citations

Mitotic errors in somatic cells cause trisomy 21 in about 4.5% of cases and are not associated with advanced maternal age

1993 • 147 citations

A somatic origin of homologous Robertsonian translocations and isochromosomes.

1994 • 127 citations

Uniparental disomy 15 resulting from "correction" of an initial trisomy 15.

1992 • 123 citations

Molecular studies of chromosomal mosaicism: relative frequency of chromosome gain or loss and possible role of cell selection.

1995 • 122 citations

Nondisjunction of human acrocentric chromosomes: studies of 432 trisomic fetuses and liveborns

1994 • 112 citations

Nondisjunction of chromosome 15: origin and recombination.

1993 • 109 citations

Uniparental isodisomy for paternal 7p and maternal 7q in a child with growth retardation.

1994 • 89 citations

Prenatal and postnatal growth failure associated with maternal heterodisomy for chromosome 7.

1995 • 86 citations

Mosaicism in chorionic villus sampling: An analysis of incidence and chromosomes involved in 2612 consecutive cases

1993 • 81 citations

PRENATAL DIAGNOSIS OF UNIPARENTAL DISOMY 15 FOLLOWING TRISOMY 15 MOSAICISM

1996 • 74 citations

Distribution of mosaicism in human placentae

1996 • 71 citations

Maternal uniparental disomy of chromosome 2 in a baby with trisomy 2 mosaicism in amniotic fluid culture

1995 • 67 citations

Mosaicism and accuracy of prenatal cytogenetic diagnoses after chorionic villus sampling and placental biopsies

1991 • 64 citations

Trisomy 7 CVS mosaicism: Pregnancy outcome, placental and DNA analysis in 14 cases

1996 • 59 citations

Normal phenotype with maternal isodisomy in a female with two isochromosomes: i(2p) and i(2q)

1996 • 58 citations

Confined Placental Mosaicism and Stillbirth

1994 • 54 citations

Confined placental mosaicism

1994 • 48 citations

Molecular studies of the aetiology of trisomy 8 in spontaneous abortions and the liveborn population

1996 • 48 citations

ANALYSIS OF NINE PREGNANCIES WITH CONFINED PLACENTAL MOSAICISM FOR TRISOMY 2

1996 • 27 citations